It is shown that Arc acts as a transcriptional repressor to directly bind the transposon’s native promoter sequence regulating TnpA and TnpB gene expression, revealing a regulatory layer that may promote long-term persistence of IS605-family elements by keeping their activity in check.
Abstract
Bacterial insertion sequences (IS) are compact transposable elements that encode proteins required for their mobility and maintenance, yet many also encode accessory proteins with poorly understood functions. For example, IS605-family elements often encode a transposase called TnpA and an RNA-guided nuclease called TnpB that supports transposon maintenance, alongside an additional ribbon-helix-helix protein named Arc. Though the roles of TnpA and TnpB have been extensively studied in recent years, the enigmatic function of Arc has not been investigated. Here, we show that Arc acts as a transcriptional repressor to directly bind the transposon’s native promoter sequence regulating TnpA and TnpB gene expression. By systematically testing Arc-containing IS605 elements, we identified a conserved binding pattern at intergenic transposon sequences neighboring protein-coding genes through chromatin immunoprecipitation and sequencing analyses. We then used fluorescence reporter assays and demonstrated that these intergenic sequences function as strong promoters, and that the presence of Arc dramatically reduces their gene expression. Together, these findings identify Arc as a transposon-encoded transcriptional repressor, revealing a regulatory layer that may promote long-term persistence of IS605-family elements by keeping their activity in check. The widespread association of Arc homologs with diverse mobile elements and cellular genes suggests that these compact regulators may more broadly restrain the expression of neighboring genetic machinery across varied genomic contexts.
TnpB nucleases, the evolutionary progenitors of CRISPR-associated Cas12 enzymes, are transposon-encoded, RNA-guided endonucleases found throughout bacteria. Independent of the trajectory towards adaptive immunity, TnpB nucleases have also recurrently given rise to TnpB-like nuclease-dead repressors (TldRs), a family of...
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Transposons were originally described as “controlling elements,” yet the molecular basis and evolutionary origin of their transcriptional regulatory activities remain elusive. Here, we show that transcriptional regulatory activity is an intrinsic property of transposases (TPases). We demonstrate that the Arabidopsis At...
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Paramutation is an interaction of alleles resulting in heritable gene silencing, but the molecular events that initiate paramutation are largely unknown. We observed unexpected silencing of the maize P1-rr gene by p1 alleles containing two nearby Ac/fAc transposable elements. A panel of derivative alleles containing th...
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Summary Programmable DNA integration using CRISPR-associated transposase elements (CASTs) offer powerful capabilities for genome engineering. The large single effector Cas12k CAST examples evolved from a minimal TnpB nuclease protein. Here, we engineer a de novo RNA-guided transposition systems in bacteria, where the s...
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It is found that BRI1 contains an exonic enhancer (EE), which is essential to establish the spatial BRI1 expression pattern, and its disruption restricts BRI1 expression and impairs BRI1-dependent root growth, linking exon-encoded regulatory information and development.
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It is shown that CpG islands in gene transcriptional start sites are typically hypomethylated and associated with higher gene expression, consistent with a host-defence role in suppressing transposition activity.
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